University of Arizona College of Pharmacy, Tucson, AZ, USA.
Ann Pharmacother. 2022 Jan;56(1):83-92. doi: 10.1177/10600280211005425. Epub 2021 Apr 8.
To review the clinical usefulness of the biomarker TIMP-2•IGFBP7 in adult, general medical-surgical intensive care unit (ICU) settings.
PubMed (1946 to mid-February 2021) and EMBASE (1947 to mid-February 2021) with bibliographies of retrieved articles reviewed for additional articles.
Studies evaluating use of the urinary TIMP-2•IGFBP7 assay in adult patients in ICU settings.
Studies published after investigations leading to TIMP-2•IGFBP7 assay approval confirm the appropriateness of considerations discussed in product labeling, such as use of the test within 12 hours of assessment, use of a dichotomous 0.3 (ng/mL)/1000 cutoff, and use only in combination with other assessments of acute kidney injury (AKI). However, as a biomarker routinely used for early identification of patients at risk for AKI in mixed ICU populations, the additional resources required for TIMP-2•IGFBP monitoring are difficult to justify because of limited data demonstrating usefulness in preventing or ameliorating AKI and its attendant complications.
Biomarkers are potentially useful not only for assessment and diagnosis of AKI, but also for practitioners involved in the management of nephrotoxic medications and medications needing adjustment for decreased kidney function.
Although there is evidence to suggest that the urinary TIMP-2•IGFBP7 biomarker is helpful in predicting AKI progression in general medical-surgical ICU patients when used within 12 hours of patient assessment in combination with routine testing, including serum creatinine and urine output, there is little evidence that its use leads to improvements in clinically important patient outcomes.
综述生物标志物 TIMP-2•IGFBP7 在成人普通内科-外科重症监护病房(ICU)环境中的临床应用价值。
PubMed(1946 年至 2021 年 2 月中旬)和 EMBASE(1947 年至 2021 年 2 月中旬),并对检索到的文章的参考文献进行了审查,以获取其他文章。
评估 ICU 成人患者尿液 TIMP-2•IGFBP7 检测应用的研究。
在 TIMP-2•IGFBP7 检测方法获得批准后发表的研究证实了产品标签中讨论的考虑因素是合理的,例如在评估后 12 小时内使用该检测、使用 0.3(ng/mL)/1000 的二值截断值以及仅与急性肾损伤(AKI)的其他评估联合使用。然而,作为一种常规用于识别混合 ICU 人群中 AKI 风险患者的生物标志物,由于缺乏数据表明 TIMP-2•IGFBP 监测在预防或改善 AKI 及其相关并发症方面的有用性,因此很难为其监测所需的额外资源提供理由。
生物标志物不仅对 AKI 的评估和诊断有潜在的作用,而且对涉及肾毒性药物管理和需要根据肾功能降低调整药物剂量的从业者也有作用。
尽管有证据表明,在患者评估后 12 小时内,将 TIMP-2•IGFBP7 尿液生物标志物与常规检测(包括血清肌酐和尿量)联合使用,有助于预测普通内科-外科 ICU 患者 AKI 的进展,但很少有证据表明其使用可改善患者的临床结局。